Demonstrates magnetic resonance imaging responsiveness in hollow microspheres, indicating a new approach for sustained drug delivery.
Hollow hydroxyapatite (HAp)‐based ceramic microspheres are attractive microcarrier architectures for integrating molecular loading, sustained release, and additional imaging responsiveness. In this study, MnFe 2 O 4 ‐incorporated hollow HAp microspheres were constructed through an improved two‐step solvothermal method to integrate MRI responsiveness and sustained model drug release within a single ceramic composite microcarrier. The obtained microspheres exhibited a hollow porous architecture, with a representative diameter of ≈1.5 μm and a shell thickness of ≈200 nm. Structural and elemental analyses confirmed the formation of hollow HAp–MnFe 2 O 4 composite microspheres with Mn‐ and Fe‐containing components distributed in the shell. The microspheres showed clear magnetic responsiveness, with a saturation magnetization of 19.45 emu g −1 , and exhibited concentration‐dependent in vitro T 2 ‐weighted MRI responsiveness with a transverse relaxivity of 39.12 mM −1 s −1 . Using metformin hydrochloride as a model drug, the microspheres achieved a drug loading efficiency of ≈63.2% and a cumulative release of 85.66% over 7 days in PBS. Live/dead staining further indicated preliminary cytocompatibility under the tested extraction/culture conditions. These results demonstrate a ceramic composite microcarrier platform integrating MRI responsiveness and sustained molecular release.
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